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Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels

AIM: High mobility group box‐1 (HMGB1) is a lethal mediator of sepsis that binds to haptoglobin (Hp) and is associated with its prognosis. We investigated the effect of the combination of HMGB1 and Hp on sepsis prognosis. METHODS: This single‐center, retrospective study registered 78 patients with s...

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Autores principales: Mizuno, Takayoshi, Eguchi, Yutaka, Tsujita, Yasuyuki, Imashuku, Yasuhiko, Tabata, Takahisa, Kitagawa, Hirotoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805693/
https://www.ncbi.nlm.nih.gov/pubmed/35127103
http://dx.doi.org/10.1002/ams2.726
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author Mizuno, Takayoshi
Eguchi, Yutaka
Tsujita, Yasuyuki
Imashuku, Yasuhiko
Tabata, Takahisa
Kitagawa, Hirotoshi
author_facet Mizuno, Takayoshi
Eguchi, Yutaka
Tsujita, Yasuyuki
Imashuku, Yasuhiko
Tabata, Takahisa
Kitagawa, Hirotoshi
author_sort Mizuno, Takayoshi
collection PubMed
description AIM: High mobility group box‐1 (HMGB1) is a lethal mediator of sepsis that binds to haptoglobin (Hp) and is associated with its prognosis. We investigated the effect of the combination of HMGB1 and Hp on sepsis prognosis. METHODS: This single‐center, retrospective study registered 78 patients with sepsis according to Sepsis‐3 criteria on day 1 of diagnosis from July 2016 to November 2018. We divided the patients into four groups according to the serum concentration of 6.2 ng/mL HMGB1 and the median value of Hp. The 180‐day mortality rates and cytokine concentrations of the low and high HMGB1 groups were compared. RESULTS: There was no difference in the 180‐day mortality rate between the low Hp group and the high Hp group in the low HMGB1 group (P = 0.691). In the high HMGB1 group, a statistically significant difference was found between the low Hp group and the high Hp group (P = 0.002). In the high HMGB1 group, high Hp was associated with a better prognosis in univariate analysis (odds ratio, 0.131; 95% confidence interval [CI], 0.027–0.629; P = 0.011), and multivariate analysis (adjusted odds ratio, 0.086; 95% CI, 0.013–0.582; P = 0.009). In addition, in the high HMGB1 group, interleukin‐8 levels were significantly higher in the low Hp group than in the high Hp group (P = 0.004). CONCLUSION: Patients with sepsis‐induced high serum HMGB1 levels and low serum Hp levels could have a poor long‐term prognosis.
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spelling pubmed-88056932022-02-04 Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels Mizuno, Takayoshi Eguchi, Yutaka Tsujita, Yasuyuki Imashuku, Yasuhiko Tabata, Takahisa Kitagawa, Hirotoshi Acute Med Surg Original Articles AIM: High mobility group box‐1 (HMGB1) is a lethal mediator of sepsis that binds to haptoglobin (Hp) and is associated with its prognosis. We investigated the effect of the combination of HMGB1 and Hp on sepsis prognosis. METHODS: This single‐center, retrospective study registered 78 patients with sepsis according to Sepsis‐3 criteria on day 1 of diagnosis from July 2016 to November 2018. We divided the patients into four groups according to the serum concentration of 6.2 ng/mL HMGB1 and the median value of Hp. The 180‐day mortality rates and cytokine concentrations of the low and high HMGB1 groups were compared. RESULTS: There was no difference in the 180‐day mortality rate between the low Hp group and the high Hp group in the low HMGB1 group (P = 0.691). In the high HMGB1 group, a statistically significant difference was found between the low Hp group and the high Hp group (P = 0.002). In the high HMGB1 group, high Hp was associated with a better prognosis in univariate analysis (odds ratio, 0.131; 95% confidence interval [CI], 0.027–0.629; P = 0.011), and multivariate analysis (adjusted odds ratio, 0.086; 95% CI, 0.013–0.582; P = 0.009). In addition, in the high HMGB1 group, interleukin‐8 levels were significantly higher in the low Hp group than in the high Hp group (P = 0.004). CONCLUSION: Patients with sepsis‐induced high serum HMGB1 levels and low serum Hp levels could have a poor long‐term prognosis. Blackwell Publishing Ltd 2022-02-01 /pmc/articles/PMC8805693/ /pubmed/35127103 http://dx.doi.org/10.1002/ams2.726 Text en © 2022 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Mizuno, Takayoshi
Eguchi, Yutaka
Tsujita, Yasuyuki
Imashuku, Yasuhiko
Tabata, Takahisa
Kitagawa, Hirotoshi
Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title_full Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title_fullStr Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title_full_unstemmed Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title_short Mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
title_sort mortality at 180‐days is affected by serum haptoglobin levels in septic patients with high magnitude serum high mobility group box‐1 levels
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805693/
https://www.ncbi.nlm.nih.gov/pubmed/35127103
http://dx.doi.org/10.1002/ams2.726
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